GB634534A - Improved process for the synthesis of hydrocarbons - Google Patents

Improved process for the synthesis of hydrocarbons

Info

Publication number
GB634534A
GB634534A GB24990/47A GB2499047A GB634534A GB 634534 A GB634534 A GB 634534A GB 24990/47 A GB24990/47 A GB 24990/47A GB 2499047 A GB2499047 A GB 2499047A GB 634534 A GB634534 A GB 634534A
Authority
GB
United Kingdom
Prior art keywords
catalyst
conversion
reactor
phase
gas
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB24990/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB634534A publication Critical patent/GB634534A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/02Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon
    • C07C1/04Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon from carbon monoxide with hydrogen
    • C07C1/0455Reaction conditions
    • C07C1/0465Reaction conditions concerning fluidisation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/08Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles
    • B01J8/12Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by gravity in a downward flow
    • B01J8/125Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by gravity in a downward flow with multiple sections one above the other separated by distribution aids, e.g. reaction and regeneration sections
    • DTEXTILES; PAPER
    • D03WEAVING
    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D23/00General weaving methods not special to the production of any particular woven fabric or the use of any particular loom; Weaves not provided for in any other single group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/74Iron group metals
    • C07C2523/745Iron

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

The synthesis of hydrocarbons and oxygenated products from carbon monoxide and hydrogen is effected by contacting in a conversion zone with a suspension of finely-divided synthesis catalyst in a gas, the concentration of <PICT:0634534/III/1> catalyst in said suspension being sufficiently low to permit conversion and resultant heat release to take place at a substantially uniform rate over an extended path of contact between reactants and catalyst, unreacted gases being withdrawn and contacted with a dense turbulent fluidized catalyst mass to effect substantial completion of the conversion. Deposition of carbon and disintegration of the catalyst, especially iron catalysts, is thereby reduced. The dilute phase conversion is preferably effected in successive stages, independently controlled as to catalyst supply, density, and temperature, up to a conversion of say 50-80 per cent, the catalyst entrained in the upward flow of gas then being carried to the final dense phase from which it may be recirculated to the dilute phase stages. Preferred catalysts contain iron obtained from oxides or sulphides and promoted with alkali oxides or halides, e.g. the reduction product of Fe2O3 95.4, Al2O3 2.6 K2O 2, and SiO2 1.4 parts by weight. Dilute phase densities of 0.5-10 lb./c. ft. may be established with superficial gas velocities of 1-20 ft./sec. with particle sizes of 5-150 m , and space velocities of 2,000-20,000 v./v./hr. of fresh feed. Dense phase densities of 20-150 lb./c. ft. are obtained with gas velocities of 0.1-3 ft./sec., and space velocities of less than 5,000 v./v./hr. Classification of particles may be effected in the dense phase and those of a narrow size range circulated to the dilute phase. Temperatures may vary for example from 500-650 DEG F. in the initial zone to 550-700 DEG F. in a subsequent zone, and 600-800 DEG F. in the final dense-phase zone. Fresh feed is supplied by lines 1 and 3 to reactor 10 and iron catalyst by stand-pipe 12 from reactor 50. Conditions are controlled to give a limited turbulence and slippage of catalyst particles, sufficient to permit efficient heat transfer to the cooling surfaces 18 while permitting carry-over of catalyst to reactor 30, to which additional catalyst may be fed by stand-pipe 32, and fresh feed gas by lines 21, 23. Product gases then pass to dense phase reactor 50 provided with conventional cooling means 48. Products pass through separator 58 and separated fines are returned by pipe 60 or lines 61, 63 as desired. Clarification of particles may be effected in packing 66 and those of desired size recycled.ALSO:<PICT:0634534/IV (b)/1> The synthesis of hydrocarbons and oxygenated products from carbon monoxide and hydrogen is effected by contacting in a conversion zone with a suspension of finely divided synthesis catalyst in a gas, the concentration of catalyst in said suspension being sufficiently low to permit conversion and resultant heat release to take place at a substantially uniform rate over an extended path of contact between reactants and catalyst, unreacted gases being withdrawn and contacted with a dense turbulent fluidized catalyst mass to effect substantial completion of the conversion. Deposition of carbon and disintegration of the catalyst, especially iron catalysts, is thereby reduced. The dilute phase conversion is preferably effected in successive stages, independently controlled as to catalyst supply, density, and temperature, up to a conversion of say 50-80 per cent, the catalyst entrained in the upward flow of gas then being carried to the final dense phase from which it may be recirculated to the dilute phase stages. Preferred catalysts contain iron obtained from oxides or sulphides and promoted with alkali oxides or halides, e.g. the reduction product of Fe2O3 95.4, Al2O3 2.6, K2O, and SiO2 1.4 parts by weight. Dilute phase densities of 0.5-10 lb./c.ft. may be established with superficial gas velocities of 1-20 ft./sec. with particle sizes of 5-150m and space velocities of 2,000-20,000 v/v/hr. of fresh feed. Dense phase densities of 20-150 lb./c.ft. are obtained with gas velocities of 0.1-3 ft./sec. and space velocities of less than 5,000 v/v/hr. Classification of particles may be effected in the dense phase and those of a narrow size range circulated to the dilute phase. Temperatures may vary for example from 500-650 DEG F. in the initial zone to 550-700 DEG F. in a subsequent zone, and 600-800 DEG F. in the final dense phase zone. Fresh feed is supplied by lines 1 and 3 to reactor 10 and iron catalyst by standpipe 12 from reactor 50. Conditions are controlled to give a limited turbulence and slippage of catalyst particles, sufficient to permit efficient heat transfer to the cooling surfaces 18 while permitting carry-over of catalyst to reactor 30, to which additional catalyst may be fed by standpipe 32, and fresh feed gas by lines 21, 23. Product gases then pass to dense phase reactor 50 provided with conventional cooling means 48. Products pass through separator 58 and separated fines are returned by pipe 60 or lines 61, 63 as desired. Classification of particles may be effected in packing 66 and those of desired size recycled.
GB24990/47A 1946-12-12 1947-09-11 Improved process for the synthesis of hydrocarbons Expired GB634534A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US715798A US2463912A (en) 1946-12-12 1946-12-12 Synthesis of hydrocarbons

Publications (1)

Publication Number Publication Date
GB634534A true GB634534A (en) 1950-03-22

Family

ID=24875525

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24990/47A Expired GB634534A (en) 1946-12-12 1947-09-11 Improved process for the synthesis of hydrocarbons

Country Status (3)

Country Link
US (1) US2463912A (en)
GB (1) GB634534A (en)
NL (1) NL66275C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2877590A1 (en) * 2004-11-09 2006-05-12 Inst Francais Du Petrole REACTIONAL DEVICE WITH SEVERAL ZONES IN A MOVABLE BED WITH APPOINTMENT IN EACH REGION OF REGENERATED OR FRESH CATALYST

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2640844A (en) * 1947-02-05 1953-06-02 Kellogg M W Co High velocity process for synthesis of organic compounds
US2506221A (en) * 1947-02-18 1950-05-02 Hydrocarbon Ressearch Inc Catalytic synthesis of hydrocarbons
US2612512A (en) * 1947-09-16 1952-09-30 Phillips Petroleum Co Process for the synthesis of hydrocarbons from carbon monoxide and hydrogen by means of a fluidized fixed-bed
US2567932A (en) * 1948-04-30 1951-09-18 Hydrocarbon Research Inc Stagewise process for the hydrogenation of carbon monoxide
US2614114A (en) * 1948-06-26 1952-10-14 Standard Oil Dev Co Hydrocarbon synthesis
US2573795A (en) * 1948-08-16 1951-11-06 Phillips Petroleum Co Hydrocarbon synthesis process
US2662911A (en) * 1948-10-01 1953-12-15 Metallgesellschaft Ag Temperature control in the catalytic hydrogenation of carbon monoxide
US2627522A (en) * 1948-10-29 1953-02-03 Standard Oil Dev Co Method and apparatus for carrying out exothermic catalytic reactions
US2680125A (en) * 1948-11-02 1954-06-01 Metallgesellschaft Ag Catalytic hydrogenation of carbon monoxide
US2671796A (en) * 1948-12-18 1954-03-09 Hydrocarbon Research Inc Hydrocarbon synthesis and apparatus therefor
US2665288A (en) * 1949-09-06 1954-01-05 Standard Oil Dev Co Process of promoting catalytic reactions in the vapor phase
US2696461A (en) * 1950-11-30 1954-12-07 Kellogg M W Co Regeneration of hydrocarbon conversion catalysts
US2819951A (en) * 1955-02-23 1958-01-14 Shell Dev Apparatus for the regeneration of catalyst
US4003712A (en) * 1970-07-29 1977-01-18 Union Carbide Corporation Fluidized bed reactor
FR2642429B1 (en) * 1989-01-31 1991-04-19 Bp Chimie Sa PROCESS AND APPARATUS FOR POLYMERIZATION OF GASEOUS OLEFINS IN A FLUIDIZED BED REACTOR
RU2342355C2 (en) * 2003-05-16 2008-12-27 Сэсол Текнолоджи (Проприетери) Лимитед Method of obtaining liquid and gaseous products from gaseous reagents
JP4731553B2 (en) * 2004-05-10 2011-07-27 サソール テクノロジー(プロプライエタリー)リミテッド Production of liquid and optionally gaseous hydrocarbons from gaseous reactants into an expanding slurry bed

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2351248A (en) * 1938-11-25 1944-06-13 Wirth Gustav Production of hydrocarbons
US2417164A (en) * 1944-11-23 1947-03-11 Standard Oil Co Hydrocarbon synthesis

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2877590A1 (en) * 2004-11-09 2006-05-12 Inst Francais Du Petrole REACTIONAL DEVICE WITH SEVERAL ZONES IN A MOVABLE BED WITH APPOINTMENT IN EACH REGION OF REGENERATED OR FRESH CATALYST
WO2006051185A1 (en) * 2004-11-09 2006-05-18 Institut Francais Du Petrole Reaction device having a number of moving bed zones with supplementing in each regenerated or fresh catalyst zone
US7611678B2 (en) 2004-11-09 2009-11-03 Institut Francais Du Petrole Multi-zone moving-bed reaction device with an addition of regenerated or fresh catalyst in each zone

Also Published As

Publication number Publication date
US2463912A (en) 1949-03-08
NL66275C (en) 1950-07-16

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